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99696-01-2

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99696-01-2 Usage

General Description

1-(4-Trifluoromethylphenyl)-2-nitroethylene is a chemical compound with the molecular formula C9H7F3NO2. It consists of a 4-trifluoromethylphenyl group attached to a nitroethylene group. 1-(4-Trifluoromethylphenyl)-2-nitroethylene is used in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. It can also serve as a reagent in the development of new synthetic compounds. Due to the presence of a nitro group, 1-(4-Trifluoromethylphenyl)-2-nitroethylene is known to be sensitive to heat and shock, and thus should be handled with care. Overall, this chemical compound plays a crucial role in the development of advanced materials and in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 99696-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99696-01:
(7*9)+(6*9)+(5*6)+(4*9)+(3*6)+(2*0)+(1*1)=202
202 % 10 = 2
So 99696-01-2 is a valid CAS Registry Number.

99696-01-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(E)-2-nitroethenyl]-4-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 1-(2-nitro-vinyl)-4-benzotrifluoride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:99696-01-2 SDS

99696-01-2Relevant articles and documents

Catalytic Asymmetric Construction of Tertiary Carbon Centers Featuring an α-Difluoromethyl Group with CF2H-CH2-NH2as the "building Block"

Gao, Fengyun,Guo, Yifei,Sun, Mengmeng,Wang, Yalan,Yang, Changyan,Wang, Yuqiang,Wang, Kairong,Yan, Wenjin

supporting information, p. 2584 - 2589 (2021/04/13)

We report here for the first time a novel difluoromethylated ketimine building block condensed by thioisatin and difluoroethylamine, offering efficient access to a broad range of enantioenriched products bearing difluoroethylamine units (27 examples, ≤98% yield, >99% ee) in the presence of quinine-derived squaramide. Further transformation of the intermediate would generate a variety of versatile functional blocks like α-difluoromethyl amines, β-amino acid, and β-diamine with retention of the enantiomeric excess at the difluoromethyl-bound carbon.

Four-Step Domino Reaction Enables Fully Controlled Non-Statistical Synthesis of Hexaarylbenzene with Six Different Aryl Groups**

Dill, Maximilian,Grau, Benedikt W.,Hampel, Frank,Jux, Norbert,Kahnt, Axel,Tsogoeva, Svetlana B.

supporting information, p. 22307 - 22314 (2021/08/25)

Hexaarylbenzene (HAB) derivatives are versatile aromatic systems playing a significant role as chromophores, liquid crystalline materials, molecular receptors, molecular-scale devices, organic light-emitting diodes and candidates for organic electronics. Statistical synthesis of simple symmetrical HABs is known via cyclotrimerization or Diels–Alder reactions. By contrast, the synthesis of more complex, asymmetrical systems, and without involvement of statistical steps, remains an unsolved problem. Here we present a generally applicable synthetic strategy to access asymmetrical HAB via an atom-economical and high-yielding metal-free four-step domino reaction using nitrostyrenes and α,α-dicyanoolefins as easily available starting materials. Resulting domino product—functionalized triarylbenzene (TAB)—can be used as a key starting compound to furnish asymmetrically substituted hexaarylbenzenes in high overall yield and without involvement of statistical steps. This straightforward domino process represents a distinct approach to create diverse and still unexplored HAB scaffolds, containing six different aromatic rings around central benzene core.

PYRROLIDINE COMPOUNDS FOR THE TREATMENT OF MALARIA

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Page/Page column 30; 31, (2020/06/19)

Pyrrolidine derivatives of formula I are used as anti-malaria agents, wherein the variables are as defined herein. Method of employing such agents in the treatment and prevention of malaria are also provided herein.

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